An incidental finding in newborn screening leading to the...

Molecular Genetics and Metabolism Reports 2020 / 03 Vol. 22

An incidental finding in newborn screening leading to the diagnosis of a patient with ECHS1 mutations

Pajares, S., López, R.M., Gort, L., Argudo-Ramírez, A., Marín, J.L., González de Aledo-Castillo, J.M., García-Villoria, J., Arranz, J.A., Del Toro, M., Tort, F., Ugarteburu, O., Casellas, M.D., Fernán
How much do you like this book?
What’s the quality of the file?
Download the book for quality assessment
What’s the quality of the downloaded files?
Volume:
22
Language:
english
Journal:
Molecular Genetics and Metabolism Reports
DOI:
10.1016/j.ymgmr.2019.100553
Date:
March, 2020
File:
PDF, 856 KB
english, 2020
Conversion to is in progress
Conversion to is failed